top of page

DHR Compilation & Verification

3 hrOrange County

Service Description

Service Description – Device Master Record (DMR) Development At Consulting QA Services, we ensure that all manufacturing instructions, specifications, and processes are complete, accurate, and compliant through our DMR Development service. Specification Review: All product drawings, material requirements, and component specifications are evaluated for clarity, completeness, and suitability for production. Process Documentation: Manufacturing procedures, assembly instructions, and inspection steps are developed and aligned with quality and regulatory standards. Equipment & Tooling Requirements: Details for calibration, setup, and operational controls are documented to support consistent manufacturing. Labeling & Packaging Documentation: All labeling, packaging, and handling guidelines are verified to ensure accuracy and compliance with device regulations. Record Maintenance: DMR documents are organized, updated, and controlled to support efficient production and regulatory traceability. Our DMR Development service ensures that your manufacturing process is clearly defined, controlled, and compliant, enabling consistent, high-quality device production.


Contact Details

  • Orange County, CA, USA

    949-795-5813

    Support@ConsultingQAservices.com


bottom of page